Canonical Allele Identifier: CA1385030593

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879163C= , CM000665.2:g.93879163C=	GRCh38
NC_000003.11:g.93598007C= , CM000665.1:g.93598007C=	GRCh37
NC_000003.10:g.95080697C=	NCBI36
NG_009813.1:g.99928G= , LRG_572:g.99928G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1644G=	ENSP00000330021.7:p.Gln548=
ENST00000394236.9:c.1644G= MANE Select	ENSP00000377783.3:p.Gln548=
ENST00000407433.6:c.1599G=	ENSP00000385794.2:p.Gln533=
ENST00000647936.1:c.1644G=	ENSP00000496822.1:p.Gln548=
ENST00000648381.1:n.1812G=
ENST00000648853.1:c.1602G=	ENSP00000497262.1:p.Gln534=
ENST00000649103.1:c.1743G=	ENSP00000497962.1:n.1743G=
ENST00000649585.1:c.587G=	ENSP00000498163.1:n.587G=
ENST00000650591.1:c.1740G=	ENSP00000497376.1:p.Gln580=
ENST00000394236.7:c.1644G=	ENSP00000377783.3:p.Gln548=
ENST00000407433.5:c.1251G=	ENSP00000385794.1:p.Gln417=
NM_000313.3:c.1644G= , LRG_572t1:c.1644G=	NP_000304.2:p.Gln548=
NM_001314077.1:c.1740G= , LRG_572t2:c.1740G=	NP_001301006.1:p.Gln580=
NM_000313.4:c.1644G= MANE Select	NP_000304.2:p.Gln548=
NM_001314077.2:c.1740G=	NP_001301006.1:p.Gln580=